Terri P. Mcveigh
Fulham Road
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 111 publications
'Truthsets' for clinical validation of large-scale functional assays: Practice recommendations from Cancer Variant Interpretation Group UK (CanVIG-UK).
Journal: medRxiv : the preprint server for health sciences
Published: July 30, 2026
Integrating enriched case data from national laboratory testing with population-based case-control analyses: a novel statistical likelihood-ratio methodology for PS4 applied to 325,345 breast cancer cases and 671,006 controls.
Journal: medRxiv : the preprint server for health sciences
Published: May 25, 2026
Cancer Variant Interpretation Group UK (CanVIG-UK): updates on an exemplar national subspecialty multidisciplinary network.
Journal: Journal of medical genetics
Published: March 22, 2026
Health-related quality of life after risk-reducing hysterectomy (PRESCORES): a cross-sectional study.
Journal: EClinicalMedicine
Published: February 15, 2026
The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.
Journal: Journal of medical genetics
Published: January 22, 2026
Somatic and germline genetic testing pathways in haematological malignancies: Best practice consensus guidelines from the 2025 national meeting organised by UK Cancer Genetics Group (UKCGG), CanGene-CanVar and the NHS England Haematological Oncology Working Group.
Journal: British journal of haematology
Published: November 14, 2025
Specific considerations for MUTYH carrier testing in individuals of Gujarati heritage: UK cancer genetics group recommendations.
Journal: Journal of medical genetics
Published: September 15, 2025
Leveraging paired germline and somatic analysis to improve the classification of DDX41 variants.
Journal: British journal of haematology
Published: September 06, 2025
Real-World Molecular Testing in European Early-Onset Colorectal Cancer.
Journal: United European gastroenterology journal
Published: July 29, 2025
Developing a germline prostate cancer risk test incorporating rare and common variants, to inform clinical decisions: a route to precision oncology.
Journal: Genome medicine
Published: July 29, 2025
Last Updated: 09/26/2026